Canonical Allele Identifier: PA2826659710
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1513070
ClinVar RCV Id: RCV002018315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala80Pro
CA342808393
NM_001282626.2:c.238G>C